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Predictors of β-blocker adherence in cardiac inherited disease

OBJECTIVE: The cardiac inherited disease (CID) population has suboptimal adherence to long-term β-blocker therapy, which is known to be a risk for sudden cardiac death. This study aimed to identify the clinical and psychosocial variables associated with non-adherence in this population. METHODS: 130...

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Autores principales: O’Donovan, Claire E, Waddell-Smith, Kathryn E, Skinner, Jonathan R, Broadbent, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307606/
https://www.ncbi.nlm.nih.gov/pubmed/30613409
http://dx.doi.org/10.1136/openhrt-2018-000877
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author O’Donovan, Claire E
Waddell-Smith, Kathryn E
Skinner, Jonathan R
Broadbent, Elizabeth
author_facet O’Donovan, Claire E
Waddell-Smith, Kathryn E
Skinner, Jonathan R
Broadbent, Elizabeth
author_sort O’Donovan, Claire E
collection PubMed
description OBJECTIVE: The cardiac inherited disease (CID) population has suboptimal adherence to long-term β-blocker therapy, which is known to be a risk for sudden cardiac death. This study aimed to identify the clinical and psychosocial variables associated with non-adherence in this population. METHODS: 130 individuals (aged 16–81 years, median: 54) from the New Zealand Cardiac Inherited Disease Registry taking β-blockers participated: 65 (50%) long QT syndrome, 42 (32%) hypertrophic cardiomyopathy and 23 (18%) other. Participants completed one questionnaire recording self-reported adherence, anxiety, depression, confidence in taking medication, illness perceptions and medication beliefs. Demographic and clinical variables were taken from the registry. RESULTS: 21 participants (16%) were classed as non-adherent. Bivariate analysis showed that self-reported adherence was worse in those who were younger (p<0.001), had a channelopathy not cardiomyopathy (p<0.01), reported lower confidence in taking β-blockers (p<0.001), had high concerns (p<0.05) and low necessity beliefs about their β-blocker (p<0.001), a poorer understanding of their CID (p<0.01), and lower treatment control beliefs (p<0.01). These variables accounted for 37% of the variance in adherence in a linear regression model. Stronger beliefs around medication necessity and higher confidence in their ability to take their medication predicted β-blocker adherence. CONCLUSIONS: Factors associated with β-blocker non-adherence in patients with CID include young age, having a channelopathy, negative medication beliefs, low confidence in taking medication and poor illness perceptions. These findings present an opportunity to develop targeted interventions to improve adherence.
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spelling pubmed-63076062019-01-04 Predictors of β-blocker adherence in cardiac inherited disease O’Donovan, Claire E Waddell-Smith, Kathryn E Skinner, Jonathan R Broadbent, Elizabeth Open Heart Arrhythmias and Sudden Death OBJECTIVE: The cardiac inherited disease (CID) population has suboptimal adherence to long-term β-blocker therapy, which is known to be a risk for sudden cardiac death. This study aimed to identify the clinical and psychosocial variables associated with non-adherence in this population. METHODS: 130 individuals (aged 16–81 years, median: 54) from the New Zealand Cardiac Inherited Disease Registry taking β-blockers participated: 65 (50%) long QT syndrome, 42 (32%) hypertrophic cardiomyopathy and 23 (18%) other. Participants completed one questionnaire recording self-reported adherence, anxiety, depression, confidence in taking medication, illness perceptions and medication beliefs. Demographic and clinical variables were taken from the registry. RESULTS: 21 participants (16%) were classed as non-adherent. Bivariate analysis showed that self-reported adherence was worse in those who were younger (p<0.001), had a channelopathy not cardiomyopathy (p<0.01), reported lower confidence in taking β-blockers (p<0.001), had high concerns (p<0.05) and low necessity beliefs about their β-blocker (p<0.001), a poorer understanding of their CID (p<0.01), and lower treatment control beliefs (p<0.01). These variables accounted for 37% of the variance in adherence in a linear regression model. Stronger beliefs around medication necessity and higher confidence in their ability to take their medication predicted β-blocker adherence. CONCLUSIONS: Factors associated with β-blocker non-adherence in patients with CID include young age, having a channelopathy, negative medication beliefs, low confidence in taking medication and poor illness perceptions. These findings present an opportunity to develop targeted interventions to improve adherence. BMJ Publishing Group 2018-12-16 /pmc/articles/PMC6307606/ /pubmed/30613409 http://dx.doi.org/10.1136/openhrt-2018-000877 Text en © Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Arrhythmias and Sudden Death
O’Donovan, Claire E
Waddell-Smith, Kathryn E
Skinner, Jonathan R
Broadbent, Elizabeth
Predictors of β-blocker adherence in cardiac inherited disease
title Predictors of β-blocker adherence in cardiac inherited disease
title_full Predictors of β-blocker adherence in cardiac inherited disease
title_fullStr Predictors of β-blocker adherence in cardiac inherited disease
title_full_unstemmed Predictors of β-blocker adherence in cardiac inherited disease
title_short Predictors of β-blocker adherence in cardiac inherited disease
title_sort predictors of β-blocker adherence in cardiac inherited disease
topic Arrhythmias and Sudden Death
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307606/
https://www.ncbi.nlm.nih.gov/pubmed/30613409
http://dx.doi.org/10.1136/openhrt-2018-000877
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